Aspine USA, Inc.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Osteo-G Bone Void Filler System Ref K031319
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aspine USA, Inc. have in the registry?
The registry currently lists 1 device for Aspine USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aspine USA, Inc.'s devices?
Among its 1 most recently registered device, Aspine USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Aspine USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Aspine USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aspine USA, Inc. in the registry?
The most recently registered devices listed for Aspine USA, Inc. include OSTEO-G BONE VOID FILLER SYSTEM.